Parexel

Senior Clinical Trial Manager (FSP)

5 days left

Company
Parexel
Location
Belgium
Salary
Competitive
Posted
19 Apr 2021
Closes
19 May 2021
Ref
67106BR
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Job Description

ExecuPharm (a Parexel Company) are currentlylooking for an experienced Senior Clinical Trial Manager to join our expanding team in Europe, this is a critical role which will allow us to continue building on our strong year on year growth whilst providing the best service to our clients.

Position Purpose:
The Senior Clinical Trial Manager position has two primary responsibilities: Execution of the clinical trial including site management functions, and management of staff (indirect) within the clinical study team.

Primary Duties:
• Act as Protocol Lead on large complex clinical trials, including Global Phase 3 trials, or several smaller clinical trials. Serve as the main point of contact for clinical site management and clinical trial site monitoring functions.
• Participate as a member on assigned cross functional study team.
• Will assist with the design and review of clinical trial protocols, informed consent, case report forms, (CRFs), Statistical Analysis Plan, and Clinical Study Report in collaboration with medical monitor, biostatistician, regulatory affairs, senior management, and other relevant groups. Participate in the Clinical Protocol Committee as appropriate.
• Create and maintain clinical trial start up documents such as the Clinical Monitoring Plan. Develop or provide clinical operations / clinical trial monitoring function input for other clinical trial start up activities, including investigational drug supply plan, research specimen plan, CRF Completion Guidelines and other plans and processes as appropriate.
• Participate in the identification, evaluation, and selection of clinical trial investigators/sites
• Manage clinical trial site monitoring team metrics (i.e. monitoring frequency and trip report completion, CRFs expected/outstanding, Source Document Verification (SDV) progress, query aging, monitoring resource requirements, etc).
• Provide support to field CRAs and may assist in the initiating, monitoring, and coordinating day-to day operations of clinical trial sites.
• Coordinate and manage vendor processes for the clinical trial site monitoring function of clinical trials including central laboratories and Clinical Research Organizations (CRO).
• Primary contact for CROs Clinical Trial Site Monitoring Team to ensure CRO's performance to the terms of contract, CFR, ICH/GCP compliance, and overall quality of work.
• Oversee research specimen collection, including accountability, monitoring, reconciliation, and shipment as needed.
• Facilitate information flow between clinical trial sites, clinical project team members and other members of the clinical operations team, external CRO or contracted members, clinical field team, vendors, and other personnel as appropriate.
• Ensure completeness of Clinical Trial Management System (CTMS) and Trial Master File (TMF) for assigned studies.
• Participate in the preparation and follow-up of in-house and on-site Client sponsored quality audits.

Qualifications

More about you
Minimum 6 + years' experience CTM or minimum 8 + years' experience SNR CTM.
Extensive global or regional clinical trial/study management experience
Oncology TA area experience desirable.
Experience running European or global studies from beginning to end.
Extensive study management/leadership experience including startup, maintenance & close out.
Experience in managing per subject costs, vendor and ancillary, and monitoring costs projections and spend.
Understands how to work with vendors to accomplish tasks.
Experience of dotted line reporting & leading CRA team functions
Experience of customizing tools for all CRA projects.

A little about us
For over 30 years, we atExecuPharm have been an industry leader in providing innovative, flexible, and customized outsourcing solutions. Our Functional Service Provider (Parexel FSP) team was established to help clients accelerate pipeline development.
With over 5,000 Global FSP resources, we partner with clients to provide tailored solutions that address their unique needs.

Why Work at Parexel

There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

That's Parexel. We're a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.

How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.